Drug profile

The FDA adverse-event record for Divested Suanovil 50

111 FDA reports name Divested Suanovil 50, a high-volume drug in the CVM extract. Species, reactions, and outcomes follow.

#740 of 2,679
by report volume (all drugs)
111
adverse-event reports
16.2%
death-coded share
Dog
most-reported species

Corpus placement

According to the FDA Center for Veterinary Medicine openFDA adverse-event extract, Divested Suanovil 50 ranks #740 of 2679 by total reports (111) and #332 of 1130 by death-coded share (16.2%). National dual: Milbemycin Oxime + Spinosad is #1 of 2679 drugs by total adverse-event reports (149,624) at death-coded-share rank 965 of 1130 drugs with at least 50 reports (2.3%); separately, Atlantic Salmon Transgenic Whole (Opafp-Ghc2 Rdna Construct Inserted Into The A-Locus In The Eo-1A Lineage) is #1 highest death-coded share at 97.8% (report rank #821).

149,624
Milbemycin Oxime + Spinosad reports (#1)
97.8%
Atlantic Salmon Transgenic Whole (Opafp-Ghc2 Rdna Construct Inserted Into The A-Locus In The Eo-1A Lineage) death share (#1)
#740
This drug, reports of 2679
#332
This drug, death share of 1130

Report volume reflects how common a breed or drug is and how often owners and vets file — not actual risk. Death-coded share ranks are limited to entries with enough reports to be meaningful. The two maps do not agree at #1.

Release-over-release change

What changed in the latest FDA data snapshot

PlainBreed reconstructed the prior snapshot from dated openFDA partitions through 2025 Q4, then compared it with the 2026-07-27 openFDA export. Divested Suanovil 50 has 111 reports now versus 111 in that prior snapshot: 0 the same number of (0.0%).

Report change
+0
Death-coded reports
+0
Death-coded share
+0.0 pts

This compares reported-event counts in two source snapshots. It does not establish a change in real-world risk, product safety, or disease incidence.

Subscribe to Divested Suanovil 50 changes

Signature read: death-coded report count at 18 is the most distinctive stamp on Divested Suanovil 50's FDA AER row.

Important: Adverse event reports do not establish that a drug caused or contributed to the event. Consult your veterinarian before making treatment decisions.
111
Total Reports
18
Deaths Reported
16.2%
Death-coded share of reports

Active Ingredients

Divested Suanovil 50

Administration Routes

UnknownOralIntramuscularImmersionAuricular (Otic)

Species Affected

Dog 89
Cattle 11
Horse 6
Cat 5

Most Affected Breeds

Retriever - Labrador 12
Terrier - Yorkshire 7
Cattle (other) 6
Shepherd Dog - German 6
Terrier - Boston 6
Pit Bull 6
Quarter Horse 6
Retriever - Golden 5
Chihuahua 5
Domestic Shorthair 5

Most Reported Reactions

Vomiting 29
Lethargy (see also Central nervous system depression in 'Neurological') 14
Seizure NOS 13
Death 11
Hyperglycaemia 10
Anorexia 9
Dehydration 8
Diarrhoea 8
Death by euthanasia 7
Elevated serum alkaline phosphatase (SAP) 7
Lack of efficacy - NOS 6
Lack of efficacy (endoparasite) - heartworm 6

Outcome Breakdown

Outcome Unknown
53 (44.9%)
Recovered/Normal
35 (29.7%)
Died
12 (10.2%)
Ongoing
9 (7.6%)
Euthanized
6 (5.1%)
Recovered with Sequela
3 (2.5%)

Divested Suanovil 50: high report volume in the FDA AER row

Read these counts as reporting volume, not risk: per our methodology, a widely-prescribed drug will rack up more raw FDA reports in a given year than a rarely-used one at an identical true rate, so we recommend comparing within similar-exposure products rather than across the full 2025 catalog.

High-volume nationwide drug peers

Two openFDA-derived peer sets for Divested Suanovil 50, both floored at ≥50 reports so the neighborhoods stay in the advertised mass.

What to do with this drug

A report does not prove a drug caused the reaction; consult a veterinarian before acting on this data.

Source: FDA Center for Veterinary Medicine openFDA Animal & Veterinary Adverse Events (CVM AER) · 2025

openFDA Animal & Veterinary Adverse Events (FDA CVM) for Divested Suanovil 50 (#740 of 2,679 by report volume); death-coded 16.2%. PlainBreed drug row · death-coded report count stamp 18 · vintage 2025.

Informational only. FDA adverse-event reports are voluntary and do not prove causation; consult a veterinarian before acting on them. Verify with FDA CVM →